Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
  • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
  • C07D239/06—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
  • C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
  • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
  • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Definitions

• the present invention relates to novel nitroenamines, a process for the preparation thereof, pesticides that contain those compounds, and their use in pest control.
• nitroenamines according to the invention correspond to formula I ##STR2## wherein R 1 is dialkylamino, alkoxy, alkenyloxy, alkoxyalkyl, alkylthioalkyl, alkoxycarbonylamino, aralkoxy, 2-thiazolyl, or an unsubstituted or substituted radical from the series alkyl, alkenyl, alkynyl, cycloalkyl and aralkyl, R 2 is nitro, cyano, hydroxy, or an unsubstituted or substituted radical from the series alkyl, cycloalkyl, alkenyl, alkynyl, aralkyl, alkoxycarbonyl, amino, dialkylamino, alkylcarbonyl, alkoxycarbonyl, alkylcarbonylamino, alkoxycarbonylamino, alkylcarbonyloxy and pyridinylmethyl, R 3 is alkyl, cycloalkyl, or an
• Preferred compounds according to the invention are those wherein R 1 is di-C 1 -C 5 alkylamino, C 1 -C 5 alkoxy, C 3 -C 5 alkenyloxy, methoxy-C 1 -C 4 alkyl, methylthio-C 1 -C 4 alkyl, ethoxycarbonylamino, C 7 -C 9 aralkoxy, 2-thiazolyl or one of the halo-substituted or unsubstituted radicals C 1 -C 5 alkyl, C 3 -C 5 -alkenyl, C 3 -C 5 alkynyl, C 3 -C 7 cycloalkyl and C 7 -C 9 aralkyl, or is C 1 -C 4 alkyl that is unsubstituted or substituted in the ⁇ - or ⁇ -position by cyano, carboxy, aminocarbonyl or by C 1 -C 5 alkoxycarbonyl, R 2 is C 1 -
• R 1 is dialkylamino, alkoxy, alkenyloxy, aralkoxy or an unsubstituted or substituted radical from the series alkyl, alkenyl, alkynyl, cycloalkyl, aralkyl and heteroarylalkyl, and each of R 2 and R 3 independently of the other is alkyl, cycloalkyl or an unsubstituted or substituted pyridinylmethyl radical.
• R 1 is di-C 1 -C 5 alkylamino, C 1 -C 5 alkoxy, C 3 -C 5 alkenyloxy, C 7 -C 9 aralkoxy or one of the halo-substituted or unsubstituted radicals C 1 -C 5 alkyl, C 3 -C 5 alkenyl, C 3 -C 5 alkynyl, C 3 -C 7 cycloalkyl or C 7 -C 9 aralkyl, or is C 1 -C 4 alkyl that is unsubstituted or substituted in the ⁇ - or ⁇ -position by cyano, carboxy or by C 1 -C 4 alkoxycarbonyl, R 2 is C 1 -C 5 alkyl, C 3 -C 7 cycloalkyl or, when R 3 is alkyl or cycloalkyl, is the radical Z ##STR4## wherein each halo-substituted or unsubstituted
• aralkyl radicals there come into consideration, for example, benzyl and 1- or 2-phenylethyl and, as aralkoxy, radicals such as benzyloxy and 1- or 2-phenylethoxy may be mentioned.
• alkyls and alkyl-containing radicals that come into consideration as substituents such as dialkylamino, alkoxy, alkoxycarbonyl, alkylthio, alkylsulfinyl, alkylsulfonyl, haloalkyl, cyanoalkyl, alkylcarbonyl, alkylcarbonylamino or alkylcarbonyloxy, may be straight-chained or branched.
• alkyls are methyl, ethyl, propyl, cyclopropyl, isopropyl, butyl, isobutyl, sec.-butyl, tert.-butyl and pentyl and the isomers thereof.
• Suitable cycloalkyls are, for example, cyclopropyl, cyclopentyl or cyclohexyl.
• halogens that come into consideration as substituents are both fluorine and chlorine and also bromine and iodine, but fluorine and chlorine are preferred.
• alkyls those having from 1 to 5 carbon atoms are preferred.
• halo-substituted C 1 -C 5 alkyls that come into consideration as substituents may be straight-chained or branched and only partially halogenated or also perhalogenated, the definitions given above applying for the halogens and the alkyls.
• substituents are inter alia methyl substituted by from one to three fluorine, chlorine and/or bromine atoms, such as, for example, CHF 2 or CF 3 ; ethyl substituted by from one to five fluorine, chlorine and/or bromine atoms, such as, for example, CH 2 CF 3 , CF 2 CF 3 , CF 2 CCl 3 , CF 2 CHCl 2 , CF 2 CHF 2 , CF 2 CFCl 2 , CF 2 CHBR 2 , CF 2 CHClF, CF 2 CHBrF or CClFCHClF; propyl or isopropyl each substituted by from one to seven fluorine, chlorine and/or bromine atoms, such as, for example, CH 2 CHBrCH 2 Br, CF 2 CHFCF 3 , CH 2 CF 2 CF 3 or CH(CF 3 ) 2 ; butyl or an isomer thereof each substituted by one or more fluorine, chlorine and
• the compounds of formula I may also be in the form of acid addition salts.
• Both organic and inorganic acids are suitable for the formation of such salts. Examples of such acids are inter alia hydrochloric acid, hydrobromic acid, nitric acid, various phosphoric acids, sulfuric acid, acetic acid, propionic acid, butyric acid, valeric acid, oxalic acid, malonic acid, maleic acid, fumaric acid, lactic acid, tartaric acid, citric acid and salicylic acid.
• R 1 is cyclopropyl, or C 1 -C 4 alkyl that is unsubstituted or substituted in the ⁇ - or ⁇ -position by cyano, carboxy or by C 1 -C 4 alkoxycarbonyl
• R 2 is pyridin-3-ylmethyl, 6-chloropyridin-3-ylmethyl, 2,6-dichloropyridin-3-ylmethyl, 5,6-dichloropyridin-3-ylmethyl, 6-trifluoromethylpyridin-3-ylmethyl or pyridin-4-ylmethyl
• each of R 3 and R 4 independently of the other is C 1 -C 5 alkyl or C 3 -C 7 cycloalkyl.
• R 2 is 6-chloropyridin-3-ylmethyl
• R 3 is methyl and R 4 is methyl, ethyl, isobutyl or cyclopropyl.
• R 1 is cyclopropyl, or C 1 -C 4 alkyl that is unsubstituted or substituted in the ⁇ - or ⁇ -position by cyano, carboxy or by C 1 -C 4 alkoxycarbonyl
• R 2 is C 1 -C 5 alkyl or C 3 -C 7 cycloalkyl
• R 3 is pyridin-3-ylmethyl, 6-chloropyridin-3-ylmethyl, 2,6-dichloropyridin-3-ylmethyl, 6-trifluoromethylpyridin-3-ylmethyl or pyridin-4-ylmethyl
• R 4 is C 1 -C 5 alkyl or C 3 -C 7 cycloalkyl.
• R 1 is cyclopropyl, or C 1 -C 4 alkyl that is unsubstituted or substituted in the ⁇ - or ⁇ -position by cyano, carboxy, methoxycarbonyl or by ethoxycarbonyl
• R 2 is methyl, ethyl, isobutyl or cyclopropyl
• R 3 is pyridin-3-ylmethyl, pyridin-4-ylmethyl or 6-chloropyridin-3-ylmethyl
• R 4 is methyl, ethyl or cyclopropyl.
• the compounds of formula I according to the invention can be prepared by reacting a nitroenamine of formula II with a primary amine of formula III and with two moles of formaldehyde ##STR6## in which formulae the radicals R 1 , R 2 , R 3 and R 4 are as defined for the compound of formula I, and isolating the reaction product.
• the present invention also relates to this process.
• the compounds of formula II are known in some cases and can be prepared by known methods, such as, for example, by reacting 1-nitro-2,2-dimethylthioethylene in stages with amines of the formulae R 2 NH 2 and R 3 NHR 4 (EP-A 302,833).
• the reaction can be carried out without solvent or in water or in an organic solvent.
• the reactions proceed within a temperature range of from 0° to the boiling point of the reaction mixture, under atmospheric or optionally elevated pressure.
• R 4 is an aryl or heteroaryl radical that is unsubstituted or substituted
• R 5 is straight-chained, branched or cyclic alkyl or alkenyl that is unsubstituted or substituted by alkoxy or by cycloalkyl, or is an unsubstituted or substituted aryl or heteroaryl radical
• X 5 is unsubstituted or alkyl-substituted methylene or a chemical bond, with the proviso that R 5 is not aryl when X 5 is a single bond, are known from DE-OS 32 32 462 as medicaments that influence the circulation, especially as agents that reduce blood pressure.
• EP-A 154 178 describes insecticidally, miticidally and nematicidally active 1-pyridinylalkyl-2-nitromethylidene-1,3-diazacycloalkanes in which the heterocycle has from 5 to 7 members. That publication relates to compounds corresponding to the formula ##STR8## wherein R is a hydrogen atom or a lower alkyl group, m is 2, 3 or 4 and n is 0, 1, 2 or 3.
• the corresponding radical of the compounds according to the invention is not a member of a perhydroimidazole or perhydropyrimidine ring.
• EP-A 247 477 describes bicyclic nitroenamines of formula I' ##STR9## having activity as pesticides.
• the compounds of formula I according to the present invention have a nitro-substituted tetrahydropyrimidine ring but, unlike those compounds, they do not contain any condensed ring systems.
• the object of the present invention was to provide further active substances for pest control.
• the compounds of formula I according to the invention are valuable active ingredients in pest control since they are well tolerated by warm-blooded animals and plants.
• the compounds of formula I are therefore suitable, for example, for controlling pests of animals and plants.
• pests belong principally to the phylum of Arthropoda, such as especially insects of the orders Lepidoptera, Coleoptera, Homoptera, Heteroptera, Diptera, Thysanoptera, Orthoptera, Anoplura, Siphonaptera, Mallophaga, Thysanura, Isoptera, Psocoptera or Hymenoptera, and arachnids of the order Acarina, e.g. mites and ticks.
• Every development stage of the pests can be controlled, i.e. the adults, pupae and nymphs, and also, especially, the larvae and eggs. It is thus possible to control effectively in particular larvae and eggs of phytopathogenic insect pests and mites in crops of ornamentals and useful plants, for example in fruit and vegetable crops, and especially in cotton crops. If compounds of formula I are ingested by imagines, then a direct kill of the pests or a reduced oviposition and/or hatching rate can be observed. The latter phenomenon can be observed especially in Coleoptera. In the control of pests that are parasites of animals, especially of domestic animals and productive livestock, the chief pests are ectoparasites, such as mites and ticks and Diptera, for example Lucilia sericata.
• the good pesticidal activity of the compounds of formula I according to the invention corresponds to a mortality of at least 50-60% of the pests mentioned above.
• the activity of the compounds of the invention and of the compositions containing them can be substantially broadened and adapted to prevailing circumstances by the addition of other insecticides and/or acaricides.
• suitable additives are representatives of the following classes of active ingredient: organophosphorus compounds, nitrophenols and derivatives thereof, formamidines, ureas, carbamates, pyrethroids, chlorinated hydrocarbons and Bacillus thuringiensis preparations.
• the compounds of formula I are used in unmodified form or, preferably, together with the inert adjuvants conventionally employed in the art of formulation and tolerated by plants, and can therefore be formulated in known manner, e.g. into emulsifiable concentrates, directly sprayable or dilutable solutions, dilute emulsions, wettable powders, soluble powders, dusts, granulates, and also encapsulations in e.g. polymer substances.
• the methods of application such as spraying, atomising, dusting, scattering or pouring, are chosen in accordance with the intended objectives and the prevailing circumstances.
• compositions i.e. the compositions, preparations or mixtures containing the active ingredient of formula I or combinations thereof with other insecticides or acaricides, and, where appropriate, a solid or liquid adjuvant
• extenders e.g. solvents, solid carriers and, where appropriate, surface-active compounds (surfactants).
• Suitable solvents are: aromatic hydrocarbons, preferably the fractions containing 8 to 12 carbon atoms, e.g. xylene mixtures or substituted naphthalenes, phthalates such as dibutyl phthalate or dioctyl phthalate, aliphatic hydrocarbons such as cyclohexane or paraffins, alcohols and glycols and their ethers and esters, such as ethanol, ethylene glycol, ethylene glycol monomethyl or monoethyl ether, ketones such as cyclohexanone, strongly polar solvents such as N-methyl-2-pyrrolidone, dimethyl sulfoxide or dimethylformamide, as well as vegetable oils or epoxidised vegetable oils, such as epoxidised coconut oil or soybean oil; or water.
• aromatic hydrocarbons preferably the fractions containing 8 to 12 carbon atoms, e.g. xylene mixtures or substituted naphthalenes, phthalates such as di
• the solid carriers used e.g. for dusts and dispersible powders are normally natural mineral fillers such as calcite, talcum, kaolin, montmorillonite or attapulgite.
• Suitable granulated adsorptive carriers are porous types, for example pumice, broken brick, sepiolite or bentonite; and suitable nonsorbent carriers are, for example, calcite or sand.
• a great number of pregranulated materials of inorganic or organic nature can be used, e.g. especially dolomite or pulverised plant residues.
• suitable surface-active compounds are non-ionic, cationic and/or anionic surfactants having good emulsifying, dispersing and wetting properties.
• surfactants shall also be understood as comprising mixtures of surfactants.
• Suitable soaps are the alkali metal salts, alkaline earth metal salts or unsubstituted or substituted ammonium salts of higher fatty acids (C 10 -C 22 ), e.g. the sodium or potassium salts of oleic or stearic acid or of natural fatty acid mixtures which can be obtained e.g. from coconut or tall oil. Mention may also be made of fatty acid methyltaurin salts and also modified and unmodified phospholipids.
• so-called synthetic surfactants are used, especially fatty sulfonates, fatty sulfates, sulfonated benzimidazole derivatives or alkylarylsulfonates.
• the fatty sulfonates or sulfates are usually in the form of alkali metal salts, alkaline earth metal salts or unsubstituted or substituted ammonium salts and contain a C 8 -C 22 alkyl radical which also includes the alkyl moiety of acyl radicals, e.g. the sodium or calcium salt of lignosulfonic acid, of dodecylsulfate or of a mixture of fatty alcohol sulfates obtained from natural fatty acids.
• acyl radicals e.g. the sodium or calcium salt of lignosulfonic acid, of dodecylsulfate or of a mixture of fatty alcohol sulfates obtained from natural fatty acids.
• These compounds also comprise the salts of sulfated and sulfonated fatty alcohol/ethylene oxide adducts.
• the sulfonated benzimidazole derivatives preferably contain 2 sulfonic acid groups and one fatty acid radical containing 8 to 22 carbon atoms.
• alkylarylsulfonates are the sodium, calcium or triethanolamine salts of dodecylbenzenesulfonic acid, dibutylnaphthalenesulfonic acid, or of a condensate of naphthalenesulfonic acid and formaldehyde.
• corresponding phosphates e.g. salts of the phosphoric acid ester of an adduct of p-nonylphenol with 4 to 14 moles of ethylene oxide.
• Non-ionic surfactants are preferably polyglycol ether derivatives of aliphatic or cycloaliphatic alcohols, saturated or unsaturated fatty acids and alkylphenols, said derivatives containing 3 to 30 glycol ether groups and 8 to 20 carbon atoms in the (aliphatic) hydrocarbon moiety and 6 to 18 carbon atoms in the alkyl moiety of the alkylphenols.
• non-ionic surfactants are the water-soluble adducts of polyethylene oxide with polypropylene glycol, ethylenediaminopolypropylene glycol and alkylpolypropylene glycol containing 1 to 10 carbon atoms in the alkyl chain, which adducts contain 20 to 250 ethylene glycol ether groups and 10 to 100 propylene glycol ether groups. These compounds usually contain 1 to 5 ethylene glycol units per propylene glycol unit.
• non-ionic surfactants are nonylphenolpolyethoxyethanols, castor oil polyglycol ethers, castor oil thioxilate, polypropylene/polyethylene oxide adducts, tributylphenoxypolyethoxyethanol, polyethylene glycol and octylphenoxypolyethoxyethanol.
• Fatty acid esters of poloxyethylene sorbitan, e.g. polyoxyethylene sorbitan trioleate are also suitable non-ionic surfactants.
• Cationic surfactants are preferably quaternary ammonium salts which contain, as N-substituent, at least one C 8 -C 22 alkyl radical and, as further substituents, unsubstituted or halogenated lower alkyl, benzyl or hydroxy-lower alkyl radicals.
• the salts are preferably in the form of halides, methylsulfates or ethylsulfates, e.g. stearyltrimethylammonium chloride or benzyldi(2-chloroethyl)ethylammonium bromide.
• the pesticidal compositions usually contain from 0.1 to 99%, preferably from 0.1 to 95%, of a compound of formula I or a combination thereof with other insecticides or acaricides, from 1 to 99.9% of a solid or liquid adjuvant, and from 0 to 25%, preferably from 0.1 to 20%, of a surfactant. Whereas commercial products will preferably be formulated as concentrates, the end user will normally employ dilute formulations of substantially lower concentration.
• compositions may also contain further auxiliaries, such as stabilisers, antifoams, viscosity regulators, binders, tackifiers as well as fertilisers or other active ingredients for obtaining special effects.
• auxiliaries such as stabilisers, antifoams, viscosity regulators, binders, tackifiers as well as fertilisers or other active ingredients for obtaining special effects.
• Example P3 Analogously to Example P3, 2.6 g of 1-nitro-2-methylamino-2-[(methyl-)(6-chloropyridin-3-ylmethyl)]-aminoethylene are reacted with 1.6 ml of ethylamine and 3.75 ml of formaldehyde and worked up. 1.7 g of the target product of m.p. 125-126° C. are isolated.
• aqueous solution of glycine methyl ester (freed from 1.5 g of glycine methyl ester hydrochloride using 0.9 ml of triethylamine in 20 ml of water and by heating at 30° C. for 15 minutes) is added to 1.5 g of 1-nitro-2-methylamino-2-[(methyl-)(5,6-dichloropyridin-3-ylmethyl)]aminoethylene suspended in 20 ml of ethanol. 1.5 ml of 37% aqueous formaldehyde are then added to the reaction mixture.
• Emulsions of any desired concentration can be produced from such concentrates by dilution with water.
• the active ingredient is dissolved in methylene chloride, the solution is sprayed onto the carrier, and the solvent is subsequently evaporated off in vacuo.
• the active ingredient is mixed and ground with adjuvants, and the mixture is subsequently moistened with water.
• the mixture is extruded and then dried in a stream of air.
• the finely ground active ingredient is uniformly applied, in a mixer, to the kaolin moistened with polyethylene glycol. Non-dusty coated granulates are obtained in this manner.
• Ready-for-use dusts are obtained by intimately mixing the carriers with the active ingredient and optionally grinding the mixture in a suitable mill.
• the active ingredient is thoroughly mixed with the adjuvants and the mixture is thoroughly ground in a suitable mill, affording wettable powders which can be diluted with water to give suspensions of the desired concentrations.
• the finely ground active ingredient is intimately mixed with the adjuvants, giving a suspension concentrate from which suspensions of any desired concentration can be obtained by dilution with water.
• the test is carried out with growing plants. For this purpose 4 rice plants (thickness of stem 8 mm) about 20 cm in height are planted into each of a number of pots (diameter 8 cm).
• each pot is sprayed on a rotary table with 100 ml of an emulsion formulation prepared from the emulsifiable concentrate of Example F1 by the addition of water and containing 400 ppm of the respective test compound.
• each plant is populated with 20 nymphs of the test organisms in the third stage.
• a glass cylinder open at both ends is slipped over each of the plants and sealed with a gauze top.
• the nymphs are kept for 10 days on the treated plant until the next development stage has been reached. Evaluation of percentage mortality is made 1, 4 and 8 days after treatment.
• Rice plants that are about 10 days old (about 10 cm high) are put into a plastics beaker that contains 20 ml of an aqueous emulsion formulation, prepared from the emulsifiable concentrate of Example Fl by the addition of water and containing the test compound in a concentration of 100 ppm, and that is sealed with a perforated plastics lid.
• the root of each rice plant is pushed through a hole in the plastic: lid into the aqueous test formulation.
• the hole is then plugged with cotton wool to fix the plant and to exclude any contact with the gas phase of the test formulation.
• the rice plant is then populated with 20 nymphs of Nilaparvata lugens in the N 2 to N 3 stage and covered with a plastics cylinder.
• test is carried out at 20° C. and 60% relative humidity and the plant is exposed to light for 16 hours. A mortality count is made 5 days later using untreated controls for comparison purposes, thereby]establishing whether the test compound absorbed through the root kills the test organisms on the upper parts of the plant.
• the test is carried out with growing plants. For :his purpose, approximately twenty-day-old rice plants about 15 cm in height are planted into each of a number of pots (diameter: 5.5 cm).
• each plant in each pot are sprayed on a rotary table with 100 ml of an acetonic solution containing 400 ppm of the test compound. After the spray coating has dried, each plant is populated with 20 nymphs of the test organisms in the second or third stage. To prevent the cicadas from escaping, a plexiglass cylinder is slipped over each of the plants and sealed with a gauze top. The nymphs are kept for 5 days on the treated plants, which have to be watered again at least once. The test is carried out at a temperature of about 23° C. and at 55% relative humidity. The plants are exposed to light for 16 hours.
• Cotton plants in the seed leaf stage are sprayed with an aqueous emulsion of active ingredient (obtained from a 10% emulsifiable concentrate) containing 400 ppm of the test compound.
• each cotton plant is populated with Spodoptera littoralis larvae in the first larval stage.
• the test is carried out at 26° C. and at about 50% relative humidity.
• a mortality count is made after 2 and 3 days, and defects in development and shedding of the larvae are determined after 5 days.
• Potted soybean plants (pot size 10 cm diameter) in the 4-leaf stage are sprayed with aqueous emulsions containing the test compound in a concentration of 400 ppm.
• the treated soybean plants are populated with 10 larvae each of Spodoptera littoralis and Heliothis virescens in the third larval stage.
• the test is carried out at 26° C. and at about 60% relative humidity in dim light. Evaluation is made 2 and 5 days later by determining the percentage mortality of the larvae.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Plural Heterocyclic Compounds (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)
• Thiazole And Isothizaole Compounds (AREA)
• Pyridine Compounds (AREA)

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• 1989
  • 1989-12-12 EP EP19890810945 patent/EP0375613A3/de not_active Withdrawn
  • 1989-12-14 US US07/450,652 patent/US5023259A/en not_active Expired - Lifetime
  • 1989-12-14 IL IL92707A patent/IL92707A0/xx unknown
  • 1989-12-19 CA CA002005977A patent/CA2005977A1/en not_active Abandoned
  • 1989-12-20 KR KR1019890019363A patent/KR900009609A/ko not_active Application Discontinuation
  • 1989-12-20 HU HU896700A patent/HUT52486A/hu unknown
  • 1989-12-20 BR BR898906609A patent/BR8906609A/pt unknown
  • 1989-12-20 AU AU47189/89A patent/AU620191B2/en not_active Ceased
  • 1989-12-20 DK DK650289A patent/DK650289A/da not_active Application Discontinuation
  • 1989-12-21 JP JP1332495A patent/JPH02258780A/ja active Pending
  • 1989-12-23 EG EG62789A patent/EG19192A/xx active

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